Canonical Allele Identifier: CA2819054038

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128031_42128032insCCCCCCAAACACACCCAACAC , CM000684.2:g.42128031_42128032insCCCCCCAAACACACCCAACAC	GRCh38
NC_000022.10:g.42524033_42524034insCCCCCCAAACACACCCAACAC , CM000684.1:g.42524033_42524034insCCCCCCAAACACACCCAACAC	GRCh37
NC_000022.9:g.40853977_40853978insCCCCCCAAACACACCCAACAC	NCBI36
NG_008376.3:g.6960_6961insGTGTTGGGTGTGTTTGGGGGG
NG_008376.4:g.7779_7780insGTGTTGGGTGTGTTTGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.691-98_691-97insGTGTTGGGTGTGTTTGGGGGG	ENSP00000353241.6:n.691-98_691-97insGTGTTGGGTGTGTTTGGGGGG
ENST00000645361.2:c.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG MANE Select	ENSP00000496150.1:n.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG
ENST00000359033.4:c.691-49_691-48insGTGTTGGGTGTGTTTGGGGGG	ENSP00000351927.4:n.691-49_691-48insGTGTTGGGTGTGTTTGGGGGG
ENST00000360124.9:c.511-98_511-97insGTGTTGGGTGTGTTTGGGGGG	ENSP00000353241.5:n.511-98_511-97insGTGTTGGGTGTGTTTGGGGGG
ENST00000360608.9:c.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG	ENSP00000353820.5:n.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG
ENST00000389970.7:c.778-49_778-48insGTGTTGGGTGTGTTTGGGGGG	ENSP00000374620.4:n.778-49_778-48insGTGTTGGGTGTGTTTGGGGGG
ENST00000488442.1:n.1568-49_1568-48insGTGTTGGGTGTGTTTGGGGGG
NM_000106.5:c.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG	NP_000097.3:n.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG
NM_001025161.2:c.691-49_691-48insGTGTTGGGTGTGTTTGGGGGG	NP_001020332.2:n.691-49_691-48insGTGTTGGGTGTGTTTGGGGGG
XM_011529966.1:c.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG	XP_011528268.1:n.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG
XM_011529967.1:c.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG	XP_011528269.1:n.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG
XM_011529968.1:c.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG	XP_011528270.1:n.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG
XM_011529969.1:c.700-49_700-48insGTGTTGGGTGTGTTTGGGGGG	XP_011528271.1:n.700-49_700-48insGTGTTGGGTGTGTTTGGGGGG
XM_011529970.1:c.691-49_691-48insGTGTTGGGTGTGTTTGGGGGG	XP_011528272.1:n.691-49_691-48insGTGTTGGGTGTGTTTGGGGGG
XM_011529971.1:c.700-49_700-48insGTGTTGGGTGTGTTTGGGGGG	XP_011528273.1:n.700-49_700-48insGTGTTGGGTGTGTTTGGGGGG
XM_011529972.1:c.843+142_843+143insGTGTTGGGTGTGTTTGGGGGG	XP_011528274.1:n.843+142_843+143insGTGTTGGGTGTGTTTGGGGGG
NM_000106.6:c.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG MANE Select	NP_000097.3:n.844-49_844-48insGTGTTGGGTGTGTTTGGGGGG
NM_001025161.3:c.691-49_691-48insGTGTTGGGTGTGTTTGGGGGG	NP_001020332.2:n.691-49_691-48insGTGTTGGGTGTGTTTGGGGGG